US2024194869A1PendingUtilityA1

Lithium nickel manganese composite oxide, positive electrode active material for lithium secondary battery, lithium secondary battery, and method of producing lithium nickel manganese composite oxide

Assignee: HONDA MOTOR CO LTDPriority: Dec 9, 2022Filed: Dec 7, 2023Published: Jun 13, 2024
Est. expiryDec 9, 2042(~16.4 yrs left)· nominal 20-yr term from priority
H01M 2004/028C01P 2002/72C01P 2006/40C01P 2002/85C01P 2002/86C01P 2002/77C01G 53/50H01M 10/052H01M 4/366H01M 4/525H01M 4/505H01M 4/36H01M 2004/021H01M 4/0471Y02E60/10
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Claims

Abstract

The present invention relates to a lithium nickel manganese composite oxide which includes secondary particles in which a plurality of primary particles are aggregated with each other, and is represented by General Formula (1): Li x Ni y Mn z O 2 (in Formula (1), x is 0.95≤x≤1.1, y is 0.45≤y≤0.5, z is 0.45≤z≤0.5, and y=z is satisfied), wherein Li contained in a transition metal layer does not form LiMn 6 , wherein the lithium nickel manganese composite oxide has a manganese-rich layer from a surface of the secondary particles toward an inside of the secondary particles, wherein a ratio of a number of Mn atoms to a number of Ni atoms (Mn/Ni ratio) in the manganese-rich layer is 1.0 or more and 1.5 or less, and wherein the lithium nickel manganese composite oxide has a space group R-3m, an a-axis lattice constant of 2.87 Å to 2.90 Å, and a c-axis lattice constant of 14.28 Å to 14.32 Å.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A lithium nickel manganese composite oxide which includes secondary particles in which a plurality of primary particles are aggregated with each other, and is represented by General Formula (1): Li x Ni y Mn z O 2  (in Formula (1), x is 0.95≤x≤1.1, y is 0.45≤y≤0.5, z is 0.45≤z≤0.5, and y=z is satisfied),
 wherein Li contained in a transition metal layer does not form LiMn 6 , 
 wherein the lithium nickel manganese composite oxide has a manganese-rich layer from a surface of the secondary particles toward an inside of the secondary particles, 
 wherein a ratio of a number of Mn atoms to a number of Ni atoms (Mn/Ni ratio) in the manganese-rich layer is 1.0 or more and 1.5 or less, and 
 wherein the lithium nickel manganese composite oxide has a space group R-3m, an a-axis lattice constant of 2.87 Å to 2.90 Å, and a c-axis lattice constant of 14.28 Å to 14.32 Å. 
 
     
     
         2 . The lithium nickel manganese composite oxide according to  claim 1 ,
 wherein, in a spectrum measured by solid-state lithium nuclear magnetic resonance analysis ( 6 Li-MAS-NMR) using a magic-angle sample rotation method, there is no peak at 1,495 to 1,505 ppm caused by LiMn 6  formed by Li contained in the transition metal layer.   
     
     
         3 . A positive electrode active material for a lithium secondary battery comprising the lithium nickel manganese composite oxide according to  claim 1  as a main component. 
     
     
         4 . A lithium secondary battery comprising a positive electrode, a negative electrode, and an electrolyte,
 wherein the positive electrode contains a positive electrode active material whose main component is the lithium nickel manganese composite oxide according to  claim 1 .   
     
     
         5 . A method of producing the lithium nickel manganese composite oxide according to  claim 1 , comprising:
 a first process in which at least one of lithium and a lithium compound is reacted with Ni a Mn b Z a , (Z is O or OH, a is 0<a<1, b is 0<b<1, a+b=1, and α is a value that keeps Ni a Mn b Z a  electrically neutral) to obtain a powder by heating a mixture containing at least one of lithium and the lithium compound, and Ni a Mn b Z a  at 950° C. or higher and 1,150° C. or lower for 1 minute or longer and 5 hours or shorter;   a second process of cooling the powder to room temperature;   a third process in which the powder is immersed in ion-exchanged water at a temperature of 50° C. or higher and 100° C. or lower for 5 minutes or longer and 3 hours or shorter;   a fourth process of drying the powder after being immersed in ion-exchanged water; and   a fifth process in which the powder after drying is heated at 800° C. or higher and 950° C. or lower for 1 hour or longer and 24 hours or shorter.

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